Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment

Introduction: Sickle Cell Anaemia (SCA) is an inherited disorder characterised by homozygosis for the mutation that causes Haemoglobin S (Hb S) production. SCA patients have increased serum levels of circulating Tumour Necrosis Factor Alpha (TNF-α) and Interleukin 8 (IL-8) during crisis events, occa...

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Main Authors: Fathelrahman M Hassan, Faisal M Alzahrani
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2018-06-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/11681/35740_CE(Ra1)_F(SS)_PF1(MJ_AP)_PN(AP).pdf
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spelling doaj-bfc5877a062f4db3a5601229d8f443d72020-11-25T02:04:11ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2018-06-01126EC14EC1710.7860/JCDR/2018/35740.11681Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea TreatmentFathelrahman M Hassan0Faisal M Alzahrani1Associate Professor, Department of Clinical Laboratory Science, College of Applied Medical Science, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.Assistant Professor, Department of Clinical Laboratory Science, College of Applied Medical Science, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.Introduction: Sickle Cell Anaemia (SCA) is an inherited disorder characterised by homozygosis for the mutation that causes Haemoglobin S (Hb S) production. SCA patients have increased serum levels of circulating Tumour Necrosis Factor Alpha (TNF-α) and Interleukin 8 (IL-8) during crisis events, occasions because of increased production from inflammatory cells, glia and neurons, these inflammatory molecules additionally contribute to the advanced mechanisms concerned in vascular occlusion events. Aim: This study aimed to investigate polymorphisms in the TNFalpha and IL-8 genes, their association with the haematological changes, to investigate the association between the TNF-alpha and IL-8 gene polymorphisms and the TNF-alpha and IL-8 serum levels in Saudi SCA patients presented with or without treatment in comparison to healthy individuals. Materials and Methods: The study included 87 SCA patients diagnosed as homozygous for Haemoglobin S (Hb S; using haemoglobin electrophoresis methods and High-Performance Liquid Chromatography (HPLC) and attended at hereditary blood disease centre (Al-Ahsa; Saudi Arabia) for follow-up. The patients of both genders in all age groups were subdivided into two groups; 27 of the patients were undergoing hydroxyurea treatment (AHU) and 60 patients without hydroxyurea treatment against 30 healthy individual setting as control group. The collected data were analysed using the STATA SE 10 and GraphPad Prism 5.0. Results: TNF-α and IL-8 levels were significantly higher within the plasma of SCA individuals compared to control individuals. The GG and AA genotypes of TNF-alpha-308G>A were associated with the increase in the serum levels of TNF-alpha in SCA patients. While, AA and TT genotypes -251A>T IL-8 gene polymorphism was associated with increase in the serum levels of IL-8 in SCA patients. Conclusion: The haematological investigations of SCA further highlight the contribution of genetic modifications to the risk of clinical genotypes to understand the association of serum levels of TNF-α and IL-8 in patients under HU compared to their gene polymorphism.https://jcdr.net/articles/PDF/11681/35740_CE(Ra1)_F(SS)_PF1(MJ_AP)_PN(AP).pdfcytokinehaemoglobin svascular occlusion
collection DOAJ
language English
format Article
sources DOAJ
author Fathelrahman M Hassan
Faisal M Alzahrani
spellingShingle Fathelrahman M Hassan
Faisal M Alzahrani
Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
Journal of Clinical and Diagnostic Research
cytokine
haemoglobin s
vascular occlusion
author_facet Fathelrahman M Hassan
Faisal M Alzahrani
author_sort Fathelrahman M Hassan
title Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
title_short Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
title_full Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
title_fullStr Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
title_full_unstemmed Cytokines TNF-Alpha and IL-8 Gene Polymorphisms in Sickle Cell Anaemia Patients under Hydroxyurea Treatment
title_sort cytokines tnf-alpha and il-8 gene polymorphisms in sickle cell anaemia patients under hydroxyurea treatment
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2018-06-01
description Introduction: Sickle Cell Anaemia (SCA) is an inherited disorder characterised by homozygosis for the mutation that causes Haemoglobin S (Hb S) production. SCA patients have increased serum levels of circulating Tumour Necrosis Factor Alpha (TNF-α) and Interleukin 8 (IL-8) during crisis events, occasions because of increased production from inflammatory cells, glia and neurons, these inflammatory molecules additionally contribute to the advanced mechanisms concerned in vascular occlusion events. Aim: This study aimed to investigate polymorphisms in the TNFalpha and IL-8 genes, their association with the haematological changes, to investigate the association between the TNF-alpha and IL-8 gene polymorphisms and the TNF-alpha and IL-8 serum levels in Saudi SCA patients presented with or without treatment in comparison to healthy individuals. Materials and Methods: The study included 87 SCA patients diagnosed as homozygous for Haemoglobin S (Hb S; using haemoglobin electrophoresis methods and High-Performance Liquid Chromatography (HPLC) and attended at hereditary blood disease centre (Al-Ahsa; Saudi Arabia) for follow-up. The patients of both genders in all age groups were subdivided into two groups; 27 of the patients were undergoing hydroxyurea treatment (AHU) and 60 patients without hydroxyurea treatment against 30 healthy individual setting as control group. The collected data were analysed using the STATA SE 10 and GraphPad Prism 5.0. Results: TNF-α and IL-8 levels were significantly higher within the plasma of SCA individuals compared to control individuals. The GG and AA genotypes of TNF-alpha-308G>A were associated with the increase in the serum levels of TNF-alpha in SCA patients. While, AA and TT genotypes -251A>T IL-8 gene polymorphism was associated with increase in the serum levels of IL-8 in SCA patients. Conclusion: The haematological investigations of SCA further highlight the contribution of genetic modifications to the risk of clinical genotypes to understand the association of serum levels of TNF-α and IL-8 in patients under HU compared to their gene polymorphism.
topic cytokine
haemoglobin s
vascular occlusion
url https://jcdr.net/articles/PDF/11681/35740_CE(Ra1)_F(SS)_PF1(MJ_AP)_PN(AP).pdf
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